Position Summary
This position may be eligible for a hybrid work arrangement that may include a partially remote work location consistent with System Office policy. UNC Chapel Hill employees are generally required to reside within a reasonable commuting distance of their assigned duty station. This position will serve as a Clinical Research Participant Coordinator within the Carolina Institute for Developmental Disabilities. The Clinical Research Participant Coordinator is responsible for research participant management and data collection for a variety of complex clinical research protocols including leading efforts in gathering compiling and reporting data. The Clinical Research Participant Coordinator facilitates the integration of research activities into the clinical care environment conveying information to a variety of individuals and groups.
Required Qualifications Competencies And Experience
Must be able to use considerable judgement and skills in performing work assignments. Strong written and verbal communication skills. Must be able to work and communicate with diverse populations effectively and professionally. Ability to work independently as well as function as part of a team. Proficient with Microsoft Outlook Excel and Word.
Preferred Qualifications Competencies And Experience
Experience in research (doesnt have to be clinical trials) and working with patient populations with developmental disorders or rare diseases.
Work Schedule
Monday Friday 8am 5pm
Required Experience:
Staff IC